Primary Device ID | M739CP300200 |
NIH Device Record Key | 877f906e-99c2-425c-8ed8-be096ac92cdd |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | 1-Level Cervical Plates, 20 mm |
Version Model Number | CP30020 |
Company DUNS | 836975784 |
Company Name | CAPTIVA SPINE, INC. |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | Labeling does not contain MRI Safety Information |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | true |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | false |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
HIBCC | M739CP300200 [Primary] |
KWQ | Appliance, Fixation, Spinal Intervertebral Body |
Steralize Prior To Use | true |
Device Is Sterile | false |
[M739CP300200]
Moist Heat or Steam Sterilization
[M739CP300200]
Moist Heat or Steam Sterilization
[M739CP300200]
Moist Heat or Steam Sterilization
[M739CP300200]
Moist Heat or Steam Sterilization
[M739CP300200]
Moist Heat or Steam Sterilization
[M739CP300200]
Moist Heat or Steam Sterilization
[M739CP300200]
Moist Heat or Steam Sterilization
[M739CP300200]
Moist Heat or Steam Sterilization
[M739CP300200]
Moist Heat or Steam Sterilization
[M739CP300200]
Moist Heat or Steam Sterilization
[M739CP300200]
Moist Heat or Steam Sterilization
[M739CP300200]
Moist Heat or Steam Sterilization
[M739CP300200]
Moist Heat or Steam Sterilization
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2023-09-18 |
Device Publish Date | 2017-08-11 |
M739CP30020 | 1-Level Cervical Plates, 20 mm |